DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 3726 - 3750 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0555198 Malignant Glioma STS 412 steroid sulfatase P08842
C1956346 Coronary Artery Disease STS 412 steroid sulfatase P08842
C4551979 Nephronophthisis 1 STS 412 steroid sulfatase P08842
C0010068 Coronary heart disease STS 412 steroid sulfatase P08842
C0037274 Dermatologic disorders STS 412 steroid sulfatase P08842
C0025286 Meningioma STS 412 steroid sulfatase P08842
C0021390 Inflammatory Bowel Diseases STS 412 steroid sulfatase P08842
C0205824 Liposarcoma, Dedifferentiated STS 412 steroid sulfatase P08842
C1844853 Brachytelephalangic Chondrodysplasia Punctata STS 412 steroid sulfatase P08842
C0039585 Androgen-Insensitivity Syndrome STS 412 steroid sulfatase P08842
C0032897 Prader-Willi Syndrome STS 412 steroid sulfatase P08842
C0009663 Condylomata Acuminata STS 412 steroid sulfatase P08842
C0036572 Seizures STS 412 steroid sulfatase P08842
C0007097 Carcinoma STS 412 steroid sulfatase P08842
C0243026 Sepsis STS 412 steroid sulfatase P08842
C0029463 Osteosarcoma STS 412 steroid sulfatase P08842
C0030409 Paracoccidioidomycosis STS 412 steroid sulfatase P08842
C0007131 Non-Small Cell Lung Carcinoma STS 412 steroid sulfatase P08842
C0023890 Liver Cirrhosis STS 412 steroid sulfatase P08842
C0085669 Acute leukemia STS 412 steroid sulfatase P08842
C0004114 Astrocytoma STS 412 steroid sulfatase P08842
C0282102 Chondrodysplasia punctata, X-linked dominant type STS 412 steroid sulfatase P08842
C0020981 Angioimmunoblastic Lymphadenopathy STS 412 steroid sulfatase P08842
C0020179 Huntington Disease STS 412 steroid sulfatase P08842
C0428791 Aortic valve calcification STS 412 steroid sulfatase P08842

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Last updated: August 19, 2024